Latest Regulatory Affairs Leader jobs in Santa Clara, CA

11 Regulatory Affairs Leader Jobs in Santa Clara, CA

Principal Clinical Research Scientist Abbott Laboratories - Santa Clara, California & Development (R&D), Regulatory Affairs, Safety and Biostatistics. Writes study protocols, protocol amendments, informed consent forms, clinical study reports, prepare scientific presentations and writes 10 days ago
Senior Research Scientist Abbott Laboratories - Santa Clara, California by interacting with study PIs, key opinion leaders (KOLs) and collaborating cross functionally with other departments including Global Clinical Operations, Research & Development, Regulatory Affairs 10 days ago
Regulatory Affairs Project Leader DivIHN Integration Inc - Santa Clara, CA one of our Talent Specialists Divya | 224 369-2969 Rashi | 630-847-1027 Title: Regulatory Affairs Project Leader Location:Santa Clara, CA Duration: 1 Year Description: Exempt/Non-Exempt: Non-exempt Education 9 days ago
Clinical Development Lead Software Guidance & Assistance, Inc. (SGA, Inc.) - Pleasanton, CA, United States on cross-functional project teams, leads the clinical development and validation strategy to register these products as In Vitro Diagnostics with regulatory agencies. The position will report to the Head 8 days ago
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Clinical Development Lead Innova Solutions - Pleasanton, CA, United States these products as In Vitro Diagnostics with regulatory agencies. The position will report to the Head of Clinical Development, Infection and Immunity, in the Clinical Development and Medical Affairs department 8 days ago
Clinical Trial Program Manager, Medical Devices Operational Compliance Center (MD-OCC) Sunnyvale, CA , Medical Devices Operational Compliance Center (MD-OCC), consists of business process analysts, quality system experts, program managers, supply chain experts, regulatory experts, clinical affairs 7 days ago
Senior Director Regulatory Affairs Meet - Redwood City, CA, United States as a cross-functional leader within the organization to facilitate prompt and accurate regulatory documentation Key Qualifications/Requirements 9+ years of Regulatory Affairs (mix of Clinical Reg and Reg CMC 15 days ago
Manufacturing Process Engineer (Medical Devices) MindSource - South San Francisco, California , Quality, Complaints and Regulatory Affairs. Regularly interact at a detailed technical level with design engineers, equipment and production engineers. Support supplier selection through assessment 2 days ago
Senior Manager - Clinical Science Abbott Laboratories - Pleasanton, California personnel in addition to working directly with physician leaders and study investigators. This position will have significant interaction with executive leadership, physicians and regulatory authorities 10 days ago
Director, Translational Sciences Allogene Therapeutics - South San Francisco, US environment interfacing with multiple functional groups including: research, clinical development, clinical and translational operations, regulatory, biometrics, bioinformatics, medical affairs More than 30 days ago

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